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Therapeutic Potential of TNF-α Inhibition for Alzheimer’s Disease Prevention
BACKGROUND: Alzheimer’s disease (AD) is increasingly prevalent and over 99% of drugs developed for AD have failed in clinical trials. A growing body of literature suggests that potent inhibitors of tumor necrosis factor-α (TNF-α) have potential to improve cognitive performance. OBJECTIVE: In this re...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7739965/ https://www.ncbi.nlm.nih.gov/pubmed/33016914 http://dx.doi.org/10.3233/JAD-200711 |
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author | Torres-Acosta, Noel O’Keefe, James H. O’Keefe, Evan L. Isaacson, Richard Small, Gary |
author_facet | Torres-Acosta, Noel O’Keefe, James H. O’Keefe, Evan L. Isaacson, Richard Small, Gary |
author_sort | Torres-Acosta, Noel |
collection | PubMed |
description | BACKGROUND: Alzheimer’s disease (AD) is increasingly prevalent and over 99% of drugs developed for AD have failed in clinical trials. A growing body of literature suggests that potent inhibitors of tumor necrosis factor-α (TNF-α) have potential to improve cognitive performance. OBJECTIVE: In this review, we summarize the evidence regarding the potential for TNF-α inhibition to prevent AD and improve cognitive function in people at risk for dementia. METHODS: We conducted a literature review in PubMed, screening all articles published before July 7, 2019 related to TNF blocking agents and curcumin (another TNF-α inhibitor) in the context of AD pathology. The keywords in the search included: AD, dementia, memory, cognition, TNF-α, TNF inhibitors, etanercept, infliximab, adalimumab, golimumab, and curcumin. RESULTS: Three large epidemiology studies reported etanercept treated patients had 60 to 70% lower odds ratio (OR) of developing AD. Two small-randomized control trials (RCTs) demonstrated an improvement in cognitive performance for AD patients treated with etanercept. Studies using animal models of dementia also reported similar findings with TNF blocking agents (etanercept, infliximab, adalimumab, Theracurmin), which appeared to improve cognition. A small human RCT using Theracurmin, a well-absorbed form of curcumin that lowers TNF-α, showed enhanced cognitive performance and decreased brain levels of amyloid-β plaque and tau tangles. CONCLUSION: TNF-α targeted therapy is a biologically plausible approach to the preservation of cognition, and warrants larger prospective RCTs to further investigate potential benefits in populations at risk of developing AD. |
format | Online Article Text |
id | pubmed-7739965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | IOS Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-77399652020-12-18 Therapeutic Potential of TNF-α Inhibition for Alzheimer’s Disease Prevention Torres-Acosta, Noel O’Keefe, James H. O’Keefe, Evan L. Isaacson, Richard Small, Gary J Alzheimers Dis Research Article BACKGROUND: Alzheimer’s disease (AD) is increasingly prevalent and over 99% of drugs developed for AD have failed in clinical trials. A growing body of literature suggests that potent inhibitors of tumor necrosis factor-α (TNF-α) have potential to improve cognitive performance. OBJECTIVE: In this review, we summarize the evidence regarding the potential for TNF-α inhibition to prevent AD and improve cognitive function in people at risk for dementia. METHODS: We conducted a literature review in PubMed, screening all articles published before July 7, 2019 related to TNF blocking agents and curcumin (another TNF-α inhibitor) in the context of AD pathology. The keywords in the search included: AD, dementia, memory, cognition, TNF-α, TNF inhibitors, etanercept, infliximab, adalimumab, golimumab, and curcumin. RESULTS: Three large epidemiology studies reported etanercept treated patients had 60 to 70% lower odds ratio (OR) of developing AD. Two small-randomized control trials (RCTs) demonstrated an improvement in cognitive performance for AD patients treated with etanercept. Studies using animal models of dementia also reported similar findings with TNF blocking agents (etanercept, infliximab, adalimumab, Theracurmin), which appeared to improve cognition. A small human RCT using Theracurmin, a well-absorbed form of curcumin that lowers TNF-α, showed enhanced cognitive performance and decreased brain levels of amyloid-β plaque and tau tangles. CONCLUSION: TNF-α targeted therapy is a biologically plausible approach to the preservation of cognition, and warrants larger prospective RCTs to further investigate potential benefits in populations at risk of developing AD. IOS Press 2020-11-10 /pmc/articles/PMC7739965/ /pubmed/33016914 http://dx.doi.org/10.3233/JAD-200711 Text en © 2020 – IOS Press and the authors. All rights reserved https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Torres-Acosta, Noel O’Keefe, James H. O’Keefe, Evan L. Isaacson, Richard Small, Gary Therapeutic Potential of TNF-α Inhibition for Alzheimer’s Disease Prevention |
title | Therapeutic Potential of TNF-α Inhibition for Alzheimer’s Disease Prevention |
title_full | Therapeutic Potential of TNF-α Inhibition for Alzheimer’s Disease Prevention |
title_fullStr | Therapeutic Potential of TNF-α Inhibition for Alzheimer’s Disease Prevention |
title_full_unstemmed | Therapeutic Potential of TNF-α Inhibition for Alzheimer’s Disease Prevention |
title_short | Therapeutic Potential of TNF-α Inhibition for Alzheimer’s Disease Prevention |
title_sort | therapeutic potential of tnf-α inhibition for alzheimer’s disease prevention |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7739965/ https://www.ncbi.nlm.nih.gov/pubmed/33016914 http://dx.doi.org/10.3233/JAD-200711 |
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